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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235585Generated: October 30, 2026

Ethyl 2-(5-fluoro-2-nitrophenoxy)acetate → 7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one

https://huagongshe.com/reaction/235585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(5-fluoro-2-nitrophenoxy)acetateHCID 13752803—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 1373129562.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

Iron powder (36.42 g) was suspended in 5% aqueous acetic acid (69 ml) and heated to 80° C. To the suspension, a solution of ethyl 5-fluoro-2-nitrophenoxyacetate (15.86 g) in acetic acid (65 ml) and ethyl acetate (65 ml) was dropwise added, and the resultant mixture was heated at 60° to 80° C. under reflux for 3 hours. After removal of residue by filtration, the filtrate was extracted with ethyl acetate. The extract was washed with water and sodium bicarbonate solution, dried and concentrated to give 7-fluoro-2H-1,4-benzoxazin-3(4H)-one (6.82 g). m.p., 186.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04640707
Source datasetuspto-grants-1987_02
ORD IDord-eff36f6230224334b85478f2010ece7d
Source noteuspto-grants-1987_02